Spine Registration Using 3D Scanning

Last updated: September 29, 2025
Sponsor: Advanced Scanners Inc.
Overall Status: Terminated

Phase

N/A

Condition

Spondylolisthesis

Ankylosing Spondylitis

Spine Athroplasty

Treatment

Optical 3D Scanner

Clinical Study ID

NCT05195580
01500
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The primary objective is to assess the capability of the device as measured by its consistency, its accuracy, and feedback from surgical staff over the study period.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patients that require exposure of bony posterior spine anatomy for localization asstandard of care.

  2. Clinically planned for spine surgery.

  3. Able to provide written informed consent from subject or subject's legalrepresentative, using IRB approved consent form, and ability for subject to complywith the protocol requirements of the study.

Exclusion

Exclusion Criteria:

  1. Language problems that would prevent from properly understanding instructions.

  2. Requirement of an interpreter.

  3. Patients who are excluded from consideration for the surgical procedure aretherefore excluded from the research study.

  4. Special populations: pregnant women, prisoners.

  5. Minimally invasive spine surgery that does not expose the necessary bone/s.

  6. Spine surgery without posterior exposure.

Study Design

Total Participants: 2
Treatment Group(s): 1
Primary Treatment: Optical 3D Scanner
Phase:
Study Start date:
August 31, 2021
Estimated Completion Date:
November 02, 2021

Connect with a study center

  • St. David's Round Rock Medical Center

    Round Rock, Texas 78681
    United States

    Site Not Available

  • St. David's Round Rock Medical Center

    Round Rock 4724129, Texas 4736286 78681
    United States

    Site Not Available

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